15 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BLACKSTONE MEDICAL INC. ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BECKMAN SYNCHRON(TM) (MICRO) TOTAL PROTEIN TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LAWRENCE L3000 CARDIAC OUTPUT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNCHRON (R) SYSTEMS CREATININE REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code CGX·July 2, 2011
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 11, 2014
OT PING METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 22, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011
BD BBL MGIT PANTA ANTIBIOTIC MIXTURE, LYOPHILIZED
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 4, 2021
BD BBL¿ MGIT¿ OADC ENRICHMENT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024
BD BBL¿ MGIT¿ OADC
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·June 3, 2025
BD BACTEC¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·July 2, 2025
BD BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·June 7, 2024
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 29, 2024
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 23, 2024
BD BBL¿ MGIT¿ OADC
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 10, 2025